PMMHRI - Familial Hypercholesterolemia Registry
NCT06571630 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2024-08-26
Summary
The registry is maintained at the Regional Centre for Rare Diseases, established in 2016, within Polish Mother's Memorial Hospital Research Institute. This facility diagnoses and treats over 80 distinct rare diseases in patients from across the country, including those with phenotypically or genetically confirmed familial hypercholesterolemia (FH).
Conditions
- Familial Hypercholesterolemia
Sponsors & Collaborators
-
Polish Mother Memorial Hospital Research Institute
lead OTHER
Eligibility
- Min Age
- 1 Day
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-01-01
- Primary Completion
- 2025-12-31
- Completion
- 2025-12-31
Countries
- Poland
Study Locations
More Related Trials
-
Familial Hypercholesterolemia Canada / Hypercholesterolemie Familiale Canada
NCT02009345 ·Status: RECRUITING
-
The Rogosin Institute Homozygous Familial Hypercholesterolemia Repository
NCT01109368 ·Status: RECRUITING
-
Screening for Familial Hypercholesterolemia in Children
NCT06555120 ·Status: RECRUITING ·Phase: NA
-
Detection of Familial Hypercholesterolaemia in Cardiovascular Disease Registry
NCT02778646 ·Status: COMPLETED
-
Study of Awareness and Detection of Familial Hypercholesterolemia
NCT01960244 ·Status: RECRUITING
-
EAS Familial Hypercholesterolaemia Studies Collaboration
NCT04272697 ·Status: RECRUITING
-
Cardiovascular Evaluation of Patients With High Cholesterol and Normal Volunteers
NCT00001204 ·Status: COMPLETED
-
Stratification of Arrhythmic Risk and/or Heart Failure Risk in Patients With Hereditary Heart Disease
NCT07257289 ·Status: RECRUITING
-
Pilot Study for a National Screening for Familial Hypercholesterolemia
NCT05271305 ·Status: UNKNOWN
-
EPIRUS FH Reverse Cascade Screening
NCT05825612 ·Status: NOT_YET_RECRUITING
-
Genetic Analysis of Familial Hypertrophic Cardiomyopathy
NCT00005251 ·Status: COMPLETED
-
Early Detection of Familial Hypercholesterolemia in Children
NCT04370899 ·Status: RECRUITING
-
The Spanish Familial Hypercholesterolaemia Cohort Study
NCT02693548 ·Status: RECRUITING
-
Familial Hypercolerstremia as Risk Factor in Stemi Patient Who Underwent Ppci
NCT03900169 ·Status: UNKNOWN
-
Human Lipoprotein Pathophysiology - Subproject: Genetics of Familial Combined Hyperlipidemia
NCT00005313 ·Status: COMPLETED
-
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease
NCT00027196 ·Status: COMPLETED
-
Registry for Mayo Clinic Adult Congenital Heart Disease Control Population
NCT05773300 ·Status: ACTIVE_NOT_RECRUITING
-
Evaluation of a Digiphysical Screening Method to Identify and Diagnose Familial Hypercholesterolemia
NCT04929457 ·Status: ENROLLING_BY_INVITATION
-
Family Heart Study (FHS)
NCT00005136 ·Status: COMPLETED
-
Natural History of Uncommon Dyslipidemias, Rare Lipid Disorders and Unusual Atherosclerotic Conditions
NCT06676046 ·Status: RECRUITING
-
High Density Lipoprotein Subspecies and Coronary Disease
NCT00005676 ·Status: COMPLETED
-
Understanding the Genetic Basis of Familial Combined Hyperlipidemia in Mexican Individuals
NCT00365235 ·Status: COMPLETED
-
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease
NCT00001881 ·Status: COMPLETED
-
Relationships Between Plasma PCSK9 Levels, LDL-cholesterol Concentrations and Lipoprotein (a) Levels in Familial Hypercholesterolemia
NCT02225340 ·Status: COMPLETED
-
Familial Hyperlipidemia Family Registry
NCT05814419 ·Status: COMPLETED